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LSMEM1 antibody (AA 31-100) (Biotin)

C7ORF53 Reactivity: Human ELISA, WB, IHC (fro), IHC (p) Host: Rabbit Polyclonal Biotin
Catalog No. ABIN1700925
  • Target See all LSMEM1 (C7ORF53) Antibodies
    LSMEM1 (C7ORF53) (Chromosome 7 Open Reading Frame 53 (C7ORF53))
    Binding Specificity
    • 14
    • 5
    AA 31-100
    Reactivity
    Human
    Host
    • 19
    Rabbit
    Clonality
    • 19
    Polyclonal
    Conjugate
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This LSMEM1 antibody is conjugated to Biotin
    Application
    • 14
    • 13
    • 13
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    ELISA, Western Blotting (WB), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Predicted Reactivity
    Human,Mouse,Rat,Dog
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C7orf53
    Isotype
    IgG
    Top Product
    Discover our top product C7ORF53 Primary Antibody
  • Application Notes
    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Preservative
    ProClin
    Precaution of Use
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C for 12 months.
    Expiry Date
    12 months
  • Target
    LSMEM1 (C7ORF53) (Chromosome 7 Open Reading Frame 53 (C7ORF53))
    Alternative Name
    C7orf53 (C7ORF53 Products)
    Synonyms
    C7orf53 antibody, Gm889 antibody, C4H7orf53 antibody, C1H7orf53 antibody, C7ORF53 antibody, leucine rich single-pass membrane protein 1 antibody, leucine-rich single-pass membrane protein 1 antibody, LSMEM1 antibody, Lsmem1 antibody
    Background

    Synonyms: C7orf53, CG053_HUMAN, Chromosome 7 open reading frame 53, Coiled-coil domain-containing transmembrane protein C7orf53.

    Background: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf53 gene product has been provisionally designated C7orf53 pending further characterization.

    Gene ID
    286006
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